A new series of (4′-hydroxy-3′,5′-dinitrophenyl) (3-aryloxiran-2-yl) methanone derivatives has been synthesized by the reaction of 4′-hydroxy-3′,5′-dinitro-substituted chalcones and alkaline H2O2. The resulted oxiranes on sulfanilic acid-catalyzed aminolysis afforded 2-hydroxy-1-(4′-hydroxy-3′,5′-dinitrophenyl)-3-aryl-3-(arylamino) propan-1-one derivatives. The advantage of this environmentally benign safe protocol offers a simple reaction set-up, mild reaction conditions, high product yields and short reaction time. The catalyst was reused several times without significant loss of catalytic activity.
Research on Chemical Intermediates – Springer Journals
Published: Jan 5, 2013
It’s your single place to instantly
discover and read the research
that matters to you.
Enjoy affordable access to
over 18 million articles from more than
15,000 peer-reviewed journals.
All for just $49/month
Query the DeepDyve database, plus search all of PubMed and Google Scholar seamlessly
Save any article or search result from DeepDyve, PubMed, and Google Scholar... all in one place.
All the latest content is available, no embargo periods.
“Whoa! It’s like Spotify but for academic articles.”@Phil_Robichaud